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Differential
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abscess, intracerebral
acquired immunodeficiency syndrome
adenine arabinoside
advances in neurology
agitation
agnosia, visual
Alzheimer's disease
Alzheimer's disease, familial
amyloid
amyloid angiopathy, cerebral
amyloid beta protein
amyloid plaques
amyotrophic lateral sclerosis, guamian type of
aneuploidy
angiitis, isolated of CNS
animal exposure
anomic aphasia
antithyroid antibodies
antiviral agents
areflexia
asymptomatic
ataxia
ataxia, cerebellar
ataxia, hereditary
ataxic gait
autoantibodies
autoimmune disease
Babinski sign
bacterial infection
basal ganglia
basal ganglia, lesion of
basal ganglia, lesion, bilateral
basilar artery occlusion
blindness
blood transfusion
bovine spongiform encephalopathy
brain biopsy
cardiac transplantation
CAT scan, abnormal
central nervous system, infection of
central pontine myelinolysis
cerebellar plaques, amyloid
cerebellum, disease of
cerebral cortex
cerebral infarction
cerebral venous infarction
cerebral venous thrombosis
cerebral venous thrombosis, deep
cerebrospinal fluid
cerebrospinal fluid, abnormal
cerebrospinal fluid, cell count
cerebrospinal fluid, elevated protein of
cerebrospinal fluid, oligoclonal IgG in
cerebrospinal fluid, protein of
cerebrovascular accident
chromosomal abnormality
Clinical Pathologic Conference(C.P.C.)
coma
concentration, impaired
confusion
corneal transplant
cortical blindness
cortical infarction
Creutzfeldt-Jakob disease, genetic
deep gray nuclei
degenerative diseases of CNS
dementia
dementia, differential diagnosis of
dementia, familial
dementia, presenile
dementia, prevention of
dementia, rapidly progressive
dementia, screening for
dementia, transmissible
dementia, treatment of
demyelinating disease
differential diagnosis
electroencephalogram
electroencephalogram, abnormalities of
electroencephalogram, periodic complexes
electroencephalogram, triphasic delta waves
electromyogram
electrophoretic pattern, CSF
encephalitis
encephalitis, bornavirus
encephalitis, viral
encephalomyelitis, postinfectious
encephalopathy
encephalopathy, Hashimoto's
encephalopathy, metabolic
endemic area
endoscopy
epidemic
epidemiology of neurology
experimental allergic encephalitis
eye movement, disorders of
Fabry's disease
familial
fatal familial insomnia
fever
flu-like illness
frontal lobe, pathologic signs of
gait disorder
gaze palsy
gaze palsy, supranuclear
gaze palsy, vertical
genetic counselling
genetic linkage
genetic neurologic disorders
Gerstmann-Straussler-Scheinker disease
glioma
growth hormone
gyrus, abnormal
Hallervorden Spatz disease
hallucination
head injury
headache
hemianopia, homonymous
hemiparesis
hepatolenticular degeneration(Wilson's disease)
herpes simplex encephalitis
herpes simplex virus
herpes virus infection
hockey stick sign
human immunodeficiency virus type 1
hyperthyroidism
hypothyroidism
hypoxic encephalopathy
iatrogenic neurologic disorders
imbalance
immunohistochemistry
incubation period
intellectual deterioration
interferon
intracerebral hemorrhage
intracerebral hemorrhage, multiple
intracerebral hemorrhage, recurrent
Jakob-Creutzfeldt disease
Jakob-Creutzfeldt disease, cerebellar variant
Jakob-Creutzfeldt disease, medical precaution with
Jakob-Creutzfeldt disease, variant
kuru
kuru plaques
lead poisoning
Leigh's disease
leukoencephalitis, acute necrotizing hemorrhagic
lymphoma involving CNS
memory, impairment of
meningitis
meningoencephalitis
mimics
misdiagnosis
mitochondrial disease
molecular genetics
mongolism
movement disorder
MRI
MRI, abnormal
MRI, abnormal, seizure causing
MRI, ADC maps
MRI, artifacts
MRI, cerebrovascular disease
MRI, demyelinating disease
MRI, diffusion weighted
MRI, early changes in CVA
MRI, false negative
MRI, FLAIR
MRI, high signal foci on
MRI, high signal intensity of basal ganglia
MRI, lesion burden
MRI, negative
MRI, T1 weighted high signal foci
multiple sclerosis
mutism
myelin
myoclonic jerks
myoclonus
myoclonus, stimulus sensitive
neoplasm, intracranial
neoplasm, primary intracerebral
neoplasm, primary of CNS
neurofibrillary degeneration
neurologic complications of, surgery
neurologic disease, diagnoses of
neurologic signs
neuronal ceroid-lipofuscinosis
neuropathology
neuropathology, brain
nystagmus
olfactory biopsy
olfactory bulb
olfactory cortex
olfactory mucosa
olfactory pathway
olfactory tract
organ donor
organ transplantation
osmotic demyelination syndrome
pain, leg
Parkinson disease
Parkinson disease, postencephalitic
PAS positive
PAS positive material in the brain
personality change
pituitary, hormones of
pleocytosis of cerebrospinal fluid
polymerase chain reaction
pons, lesion of
postictal encephalopathy
preclinical
pregnancy, neurologic complications in
prevention of neurologic disorders
prion disease
prognosis
progressive infantile poliodystrophy
progressive multifocal leucoencephalopathy
progressive neurologic disorder
protein 14-3-3, cerebrospinal fluid
psychiatric problems in neurologic disorders
psychosis
pulvinar sign
rapidly fatal neurologic illness
rapidly progressing neurologic illness
remote effect of cancer on the nervous system
review article
risk factors
sarcoidosis, CNS
scrapie
seizure
senile plaques
slow virus infection of CNS
spongy degeneration of brain
startle myoclonus
startle reaction
steroid
steroid therapy, CNS treatment and complications with
subacute sclerosing panencephalitis(S.S.P.E.)Dawson's disease
symmetric brain lesions
thalamic tumors
thalamic tumors, bilateral
thalamus
thalamus, infarction of
thalamus, infarction, bilateral
thalamus, lesion of
thalamus, lesion of-bilateral
thyroiditis
tonsil biopsy
toxic encephalopathy
trauma
treatment of neurologic disorder
tremor
tremor, intention
tuberous sclerosis
upgaze, paralysis of
urinary incontinence
viral infection
viral infection, CNS
virus, slow
vision, blurred
visual acuity, decreased
visual field defect
visual impairment
visual loss
walking, difficulty with
Wernicke's encephalopathy
West Nile fever
Western immunoblot test
Showing articles 50 to 100 of 4330 << Previous Next >>

Transissible Dementias:Current Problems in Tissue Handling
Neurol 30:302-303, Baringer,J.R.,et al, 1980

Evidence For & Against the Transmissibility of Alzheimer Disease
Neurol 30:945-950, Goudsmit,J.,et al, 1980

Presenile Alzheimer Disease:Amyloid Plaques in the Cerebellum
Neurol 30:820-825, Pro,J.D.,et al, 1980

Failure of Interferon to Modify Creutzfeldt-Jakob Disease
BMJ 280:902, Kovanen,J.,et al, 1980

Clin. Path. Conference
Creutzfeldt-Jakob Disease, Ataxic Type, with Kuru Plaques, Case Record 45-1980, NEJM 303:1162-11710., , 1980

Alzheimer Neurofibrillary Tangles in Diseases Other Than Senile & Presenile Dementia
Ann Neurol 5:288-294, Wisniewski,K.,et al, 1979

Creutzfeldt-Jakob Disease:Patterns of Worldwide Occurrence & the Significance of Familial & Sporadic Clustering
Ann Neurol 5:177-188, Masters,C.L.,et al, 1979

Studies in Aging of the Brain:IV. Familial Alzheimer Dis. :Relat. to Transmiss. Demetia, Aneuploidy, & Microtubular Defects
Neurol 29:1402, Book,R.H.,et al, 1979

Subacute Spongiform Encephalopathy (Creutzfeldt-Jakob Disease)
Brain 101:333-344, Masters,C.L.,et al, 1978

Precautions in Familial Transmissible Dementia
Arch Neurol 35:697-698, Cook,R.,et al, 1978

Precautions in Medical Care Handling Matrl. of Patients with Transmissible Virus Dementia (Creutzfeldt-Jakob Disease)
NEJM 297:1253, Gajdusek,C.,et al, 1977

Clinical Pathologic Conference, Creutzfeldt-Jakob Disease, (Case record 43-1977)
NEJM 297:930, Scully,R.E.,et al, 1977

Viral Infections & Demylinating Diseases
NEJM 288:1103, Weiner,J.,et al, 1973

Punctate Diffuse Cortex Signals in Creutzfeldt-Jakob Disease
JAMA Neurol 81:291-292, Chen,Z.,et al, 2024

Roving Eye and Head in a Patient with Genetic Creutzfeldt-Jakob Disease
Neurol 102:e209385, Nishida,K.,, 2024

Neurosyphilis Presenting as Syndrome of Limbic Encephalitis Mimicking Herpes Simplex Virus Neuro-Infection Diagnosed Using CXCL13 Point-of-Care Assay-Case Report
Brain Sci 13:503, Maresova,E.,et al, 2023

Pachymeningitis and Aortitis as the Initial Presentation of Granulomatosis with Polyangiitis
Neurol 101:979-980, Li,X.,et al, 2023

A Young Woman with Rapidly Progressive Weakness and Paresthesia
Neurol 101:676-681, Alwakeel,S.S.,et al, 2023

Rapidly Progressive Dementia in a Man With HIV Infection and Undetectable Plasma Viral Load
Neurol 100:344-348, Chishimba,L.C.,et al, 2023

More Than a Little Unsteady
NEJM 387:e9, Kraft, A.W.,et al, 2022

A 68-Year-Old Man with Palmar Rash, Leg Pain, and Inability to Walk
Neurol 99:347-353, YoungHun, J.,et al, 2022

Clinicopathologic Conference, Neurosyphilis
NEJM 386:583-590, Case 4-2022, 2022

Clinicopathologic Conference, Genetic Creutzfeldt-Jakob Disease
NEJM 386;674-687, Case 5-2022, 2022

Laboratory Diagnosis of Creutzfeldt-Jakob Disease
NEJM 386:1345-1350, Zerr, I., 2022

A 72-Year-Old Woman with Rapidly Progressive Bilateral Hearing Loss
Neurol 98:632-637, Alsalem, A.,et al, 2022

Chronic Meningitis
NEJM 385:930-936, Aksamit, A.J., 2021

Frequency and Characterization of Movement Disorders in Anti-IgLON5 Disease
Neurol 97:e1367-e1381, Gaig, C.,et al, 2021

Sporadic Creutzfeldt-Jakob Disease in a Very Young Person
Neurol 97:813-816,801, Appleby, B.S.,et al, 2021

Complete Evaluation of Dementia: PET and MRI Correlation and Diagnosis for the Neuroradiologist
AJNR 42:998-1007, Oldan, J.D.,et al, 2021

A 29-Year-Old Man with Fevers and Rapidly Progressive Cranial Neuropathies
Neurol 97:95-98, Dessy, A.,et al, 2021

A 64-Year-Old Man with Multiple Cranial Neuropathies
Neurol 97:e215-e221, Lefland, A.,et al, 2021

A 57-Year-Old Woman with Progressive Ataxia and Falls
Neurol 95:650-656, Badahdah, A., 2020

An Atypical Presentation of Creutzfeldt-Jakob Disease with a Heidenhain Variant and Balints Syndrome
Cureus DOI:10.7759/cureus,8608, Gupta,A. & Dhingra,A., 2020

Dressing Apraxia as Initial Manifestation of Creutzfeldt-Jakob Disease
Tremor and Other Hyperkinetic Movements 10:1-3, Heckmann, J.G.,et al, 2020

Variant Creutzfeldt-Jakob Disease Diagnosed 7.5 Years after Occupational Exposure
NEJM 383:83-85, Brandel, J.P.,et al, 2020

Rapid Progression of Prion Disease Associated with Transverse Myelitis
Neurol 94:e1670-e1672, Hussein, O.,et al, 2020

Pediatric Leigh Syndrome
Ann Neurol 88:218-232, Alves, C.A.P.F.,et al, 2020

A 45-Year-Old Man with Progressive Insomia and Psychiatric and Motor Symptoms
Neurol 94:e1213-e1218, Lima, J.E.E.,et al, 2020

Immunocompetent Patient with Multiple Cranial Nerve Palsies, Ataxia, and Cognitive Decline
Neurol 94:e225-e229, Nigam, M.,et al, 2020

Rapidly Progressive Gait Disorder and Cranial Nerves Involvement in a 9-year-old boy
Neurol 94:e330-e334, Lipp, A.,et al, 2020

A Rare Presentation of Whipple Disease
Neurol 94:e758-e761, Koek, A.T.,et al, 2020

Homonymous Hemianopia with Normal Magnetic Resonance Imaging
JAMA Ophthalmol doi:10.1001/JAMAOphthalmol.2020.0447, Cai, S.,et al, 2020

Long Survival Sporadic Creutzfeldt-Jakob Disease
Neurol 95:87-88, Liu, X.Y.,et al, 2020

Challenging Diagnosis of Gerstmann-Straussler-Scheinker Disease
Neurol 92:101-103, Kang, M.J.,et al, 2019

Clinicopathologic Conference, Ocular Syphilis
NEJM 380:1062-1071, Case 8-2019, 2019

Childhood Primary Angiitis of the Central Nervous System
www.UptoDate.com, Dec, Twilt, M. & Benseler, S., 2019

Neurosyphilis
NEJM 381:1358-1363, Ropper, A.H.,et al, 2019

Clinicopathologic Conference, Adenovirus Meningoencephalitis
NEJM 381:1459-1470, Case 31-2019, 2019

Clinicopathologic Conference, Creutzfeldt-Jakob Disease
NEJM 381:1569-1578, Case 32-2019, 2019

Chronic Dengue Virus Panencephalitis in a Patient with Progressive Dementia with Extrapyramidal Features
Ann Neurol 86:695-703, Johnson, T.P.,et al, 2019



Showing articles 50 to 100 of 4330 << Previous Next >>